Cladistic analysis and taxonomic review of the millipede tribe Arthrosolaenomeridini Hoffman, 1976 (Polydesmida: Chelodesmidae)

Zootaxa ◽  
2021 ◽  
Vol 4970 (2) ◽  
pp. 201-256
Author(s):  
RODRIGO SALVADOR BOUZAN ◽  
LUIZ FELIPE M. INIESTA ◽  
ANTONIO DOMINGOS BRESCOVIT

Chelodesmidae is one of the most diverse families belonging to the Polydesmida, comprising almost 800 described species distributed in 172 genera, 20 tribes and two subfamilies. Among the tribes within the Neotropical subfamily Chelodesminae, Arthrosolaenomeridini represents a very interesting group occurring in the Central-West region of Brazil. Currently the tribe contains three genera: Arthrosolaenomeris Schubart, 1943, Gangugia Schubart, 1947, and Angelodesmus Schubart, 1962. In this study, we conducted a cladistic analysis including 18 species of Arthrosolaenomeridini and 7 species of other associated Chelodesminae tribes as an outgroup. The matrix is composed of 64 morphological characters from which 39 are herein proposed for the first time. The data were analyzed under the parsimony criterion using TNT 1.5. Based on the results, Arthrosolaenomeridini was recovered as monophyletic with Macrocoxodesmini + Telonychopodini as sister group. Arthrosolaenomeris Schubart, 1943 and Gangugia Schubart, 1947 were recovered as monophyletics. The genus Angelodesmus Schubart, 1962 was recovered as paraphyletic and redefined as monotypic. The tribe is now composed of the genera Arthrosolaenomeris (6 spp.), Gangugia (6 spp.), Angelodesmus (monotypic), Abiliodesmus n. gen. (4 spp.) and Folcloredesmus n. gen. (monotypic). In addition, we conduct a taxonomic revision of the tribe Arthrosolaenomeridini providing detailed redescriptions, drawings, and distribution maps for all species and genera, including the two new genera and the ten new species proposed: Arthrosolaenomeris saci n. sp.; A. curupira n. sp.; A. caipora n. sp.; A. iara n. sp.; Gangugia boitata n. sp.; G. cuca n. sp.; G. boto n. sp.; G. mula n. sp.; Abiliodesmus mapinguari n. sp. and Folcloredesmus thomasi n. sp. Furthermore, we include an identification key to all the genera and species. 

Zootaxa ◽  
2020 ◽  
Vol 4886 (1) ◽  
pp. 1-77
Author(s):  
RICARDO ANTONIO GONÇALVES ◽  
ANTONIO DOMINGOS BRESCOVIT

A taxonomic revision and phylogenetic analysis of the spider genus Epicratinus Jocqué & Baert, 2005 is presented. The phylogenetic analysis is based on a data set including 16 Epicratinus species plus 9 outgroups representing by five related zodariid gen­era and one of them considered most basal as the root. These taxa were scored for 49 morphological characters. Parsimony was used as the op­timality criterion and a sensitivity analysis was performed using different character weighting concavities. Five unambiguous synapomorphies support the monophyly of Epicratinus. Some internal clades within the genus are well-supported and their relationships are discussed. Epicratinus includes 16 species, all with males and females. A species identification key and distribution maps are provided for all. New morphological data are also pre­sented for five previously described species. All 16 species occur only in the New World. The following species are transferred to Epicratinus: E. perfidus (Jocqué & Baert), comb. nov. from Tenedos; Epicratinus perfidus Jocqué & Baert comb. nov. and newly synonymized with E. santacruz Grismado & Izquierdo and this last species is treated as the junior synonym. Epicratinus petropolitanus (Mello-Leitão) has the male described for the first time. The following 11 species are newly described as new: E. zangief sp. nov.; E. pegasus sp. nov.; E. pikachu sp. nov.; E. stitch sp. nov.; E. ehonda sp. nov.; E. anakin sp. nov.; E. vader sp. nov.; E. omegarugal sp. nov.; E. zelda sp. nov.; E. dookan sp. nov. and E. mauru sp. nov., all from Brazil. 


2013 ◽  
Vol 27 (1) ◽  
pp. 129
Author(s):  
Edilson Caron ◽  
Cibele S. Ribeiro-Costa ◽  
Alfred F. Newton

Rove beetles of the genus Piestus Gravenhorst, 1806 are commonly captured under the bark of or inside decaying logs from Neotropical forests. Piestus belongs to the subfamily Piestinae, historically an ill-defined dumping-ground for Staphylinidae defined by plesiomorphic characters, but which has gradually been restricted in concept and currently includes only six additional extant genera worldwide. Piestinae in this restricted sense has been considered a probably monophyletic subfamily, but its status and phylogenetic position, as a possible sister-group of Osoriinae within the recently proposed Oxyteline group of staphylinid subfamilies, are uncertain and need confirmation. The main aim of the present study was to provide a morphological cladistic analysis and complete taxonomic revision of Piestus, which, as the type and most speciose genus of Piestinae, is critical for future phylogenetic studies involving the subfamily. In our study, the monophyly of Piestus is established and phylogenetic relationships among its species are proposed based on 70 adult morphological characters. Piestus is supported by 11 synapomorphies and high branch support. All species of Piestus are revised and the genus is redefined. The genus contains 43 species, including 13 species described here for the first time. The previously proposed subgenera Antropiestus Bernhauer, 1917, Eccoptopiestus Scheerpeltz, 1952, Elytropiestus Scheerpeltz, 1952, Lissopiestus Scheerpeltz, 1952, Piestus s. str., Trachypiestus Scheerpeltz, 1952 and Zirophorus Dalman, 1821 have not been confirmed, as they were found to be poly- or paraphyletic, or are here removed from Piestus, and therefore subgenera are not used. The main taxonomic changes are as follows. Lissopiestus, syn. nov. is proposed as new synonym of Eleusis Laporte, 1835 and its species, E. interrupta (Erichson, 1840), comb. rest., is transferred again to that genus. Antropiestus, syn. nov. and Eccoptopiestus, syn. nov. are proposed as new synonyms of Hypotelus Erichson, 1839 and their species, H. laevis (Solsky, 1872), comb. nov. and H. andinus (Bernhauer, 1917), comb. nov., are transferred to Hypotelus. Fourteen new synonymies are proposed (valid species listed first): P. lacordairei Laporte, 1835 = Z. furcatus Sharp, 1887, syn. nov.; P. capricornis Laporte, 1835 = P. frontalis Sharp, 1876, syn. nov.; P. pennicornis Fauvel, 1864 = P. plagiatus Fauvel, 1864, syn. nov.; P. rectus Sharp, 1876, syn. nov.; P. pygialis Fauvel, 1902, syn. nov.; P. surinamensis Bernhauer, 1928, syn. nov.; P. minutus Erichson, 1840 = P. nigrator Fauvel, 1902, syn. nov.; P. sulcatus Gravenhorst, 1806 = P. sanctaecatharinae Bernhauer, 1906, syn. nov.; P. condei Wendeler, 1955, syn. nov.; P. gounellei Fauvel, 1902 = P. wasmanni Fauvel, 1902, syn. nov.; P. mexicanus Laporte, 1835 = P. alternans Sharp, 1887, syn. nov.; P. aper Sharp, 1876 = P. schadei Scheerpeltz, 1952, syn. nov.; P. angularis Fauvel, 1864 = P. crassicornis Sharp, 1887, syn. nov.; H. andinus (Bernhauer, 1917) = P. strigipennis Bernhauer, 1921, syn. nov. One species is revalidated: P. fronticornis (Dalman, 1821), stat. rev., and one synonym is restored: P. penicillatus (Dalman, 1821) = P. erythropus Erichson, 1840, syn. rest. Neotypes are designated for P. lacordairei Laporte, 1835 and Oxytelus bicornis Olivier, 1811, and lectotypes are designated for P. puncticollis Fauvel, 1902, P. capricornis variety muticus Fauvel, 1902, P. zischkai Scheerpeltz, 1951, P. pennicornis Fauvel, 1864, P. plagiatus Fauvel, 1864, P. pygmaeus Laporte, 1835, P. niger Fauvel 1864, P. minutus Erichson, 1840, P. nigratror Fauvel, 1902, P. sulcatus Gravenhorst, 1806, P. sanctaecatharinae Bernhauer, 1906, P. sulcipennis Scheerpeltz, 1952, P. aper Sharp, 1876, P. schadei Scheerpeltz, 1952 and P. andinus Bernhauer, 1917.


ZooKeys ◽  
2018 ◽  
Vol 761 ◽  
pp. 1-177 ◽  
Author(s):  
Ruttapon Srisonchai ◽  
Henrik Enghoff ◽  
Natdanai Likhitrakarn ◽  
Somsak Panha

The dragon millipede genusDesmoxytess.l. is split into five genera, based on morphological characters and preliminary molecular phylogenetic analyses. The present article includes a review ofDesmoxytess.s., while future articles will deal withHylomusCook and Loomis, 1924 and three new genera which preliminarily are referred to as the ‘acantherpestes’, ‘gigas’, and ‘spiny’ groups. Diagnostic morphological characters of each group are discussed.Hylomusis resurrected as a valid genus and the following 33 species are assigned to it:H.asper(Attems, 1937),comb. n.,H.cattienensis(Nguyen, Golovatch & Anichkin, 2005),comb. n.,H.cervarius(Attems, 1953),comb. n.,H.cornutus(Zhang & Li, 1982),comb. n.,H.dracoCook & Loomis, 1924,stat. rev.,H.enghoffi(Nguyen, Golovatch & Anichkin, 2005),comb. n.,H.eupterygotus(Golovatch, Li, Liu & Geoffroy, 2012),comb. n.,H.getuhensis(Liu, Golovatch & Tian, 2014),comb. n.,H.grandis(Golovatch, VandenSpiegel & Semenyuk, 2016),comb. n.,H.hostilis(Golovatch & Enghoff, 1994),comb. n.,H.jeekeli(Golovatch & Enghoff, 1994),comb. n.,H.lingulatus(Liu, Golovatch & Tian, 2014),comb. n.,H.laticollis(Liu, Golovatch & Tian, 2016),comb. n.,H.longispinus(Loksa, 1960),comb. n.,H.lui(Golovatch, Li, Liu & Geoffroy, 2012),comb. n.,H.minutuberculus(Zhang, 1986),comb. n.,H.nodulosus(Liu, Golovatch & Tian, 2014),comb. n.,H.parvulus(Liu, Golovatch & Tian, 2014),comb. n.,H.phasmoides(Liu, Golovatch & Tian, 2016),comb. n.,H.pilosus(Attems, 1937),comb. n.,H.proximus(Nguyen, Golovatch & Anichkin, 2005),comb. n.,H.rhinoceros(Likhitrakarn, Golovatch & Panha, 2015),comb. n.,H.rhinoparvus(Likhitrakarn, Golovatch & Panha, 2015),comb. n.,H.scolopendroides(Golovatch, Geoffroy & Mauriès, 2010),comb. n.,H.scutigeroides(Golovatch, Geoffroy & Mauriès, 2010),comb. n.,H.similis(Liu, Golovatch & Tian, 2016),comb. n.,H.simplex(Golovatch, VandenSpiegel & Semenyuk, 2016),comb. n.,H.simplipodus(Liu, Golovatch & Tian, 2016),comb. n.,H.specialis(Nguyen, Golovatch & Anichkin, 2005),comb. n.,H.spectabilis(Attems, 1937),comb. n.,H.spinitergus(Liu, Golovatch & Tian, 2016),comb. n.,H.spinissimus(Golovatch, Li, Liu & Geoffroy, 2012),comb. n.andH.variabilis(Liu, Golovatch & Tian, 2016),comb. n.Desmoxytess.s. includes the following species:D.breviverpaSrisonchai, Enghoff & Panha, 2016;D.cervina(Pocock,1895);D.delfae(Jeekel, 1964);D.desSrisonchai, Enghoff & Panha, 2016;D.pinnasqualiSrisonchai, Enghoff & Panha, 2016;D.planata(Pocock, 1895);D.purpuroseaEnghoff, Sutcharit & Panha, 2007;D.takensisSrisonchai, Enghoff & Panha, 2016;D.taurina(Pocock, 1895);D.terae(Jeekel, 1964), all of which are re-described based mainly on type material. Two new synonyms are proposed:DesmoxytespterygotaGolovatch & Enghoff, 1994,syn. n.(=Desmoxytescervina(Pocock, 1895)),DesmoxytesrubraGolovatch & Enghoff, 1994,syn. n.(=Desmoxytesdelfae(Jeekel, 1964)). Six new species are described from Thailand:D.aurataSrisonchai, Enghoff & Panha,sp. n.,D.corythosaurusSrisonchai, Enghoff & Panha,sp. n.,D.eurosSrisonchai, Enghoff & Panha,sp. n.,D.flabellaSrisonchai, Enghoff & Panha,sp. n.,D.golovatchiSrisonchai, Enghoff & Panha,sp. n.,D.octoconigeraSrisonchai, Enghoff & Panha,sp. n., as well as one from Malaysia:D.perakensisSrisonchai, Enghoff & Panha,sp. n., and one from Myanmar:D.waepyanensisSrisonchai, Enghoff & Panha,sp. n.The species can mostly be easily distinguished by gonopod structure in combination with other external characters; some cases of particularly similar congeners are discussed. All species ofDesmoxytess.s. seem to be endemic to continental Southeast Asia (except the ‘tramp’ speciesD.planata). Some biological observations (relationship with mites, moulting) are recorded for the first time. Complete illustrations of external morphological characters, an identification key, and distribution maps of all species are provided.


2008 ◽  
Vol 22 (6) ◽  
pp. 627 ◽  
Author(s):  
Guilherme Cunha Ribeiro

Tipulomorpha (crane flies) comprise one of the largest subgroups of Diptera, but its phylogeny at different levels has been poorly explored. This study presents the most comprehensive cladistic analysis of the group ever made, with emphasis on the genera and subgenera of the subfamily Limnophilinae (Limoniidae), assumed to include some of the earliest lineages of Tipulomorpha sensu stricto and therefore important for the understanding of the early patterns in the evolution of the crane flies. Eighty-eight characters of the male imago were scored for 104 exemplar species. The most parsimonious trees were searched using implied weighting, in the framework of a sensitivity analysis with different values of k (2 to 6). The dataset based on the characters of adult male morphology showed high levels of homoplasy and yielded very incongruent and unstable phylogenetic results, which are very sensitive to changes in analytical parameters. In the preferred and most parsimonious phylogenetic hypothesis, the Pediciidae is the sister-group of all other Tipulomorpha sensu stricto. The results indicate the paraphyly of the Limoniidae with respect to the Cylindrotomidae and Tipulidae, which are considered sister-groups. The Limoniidae subfamilies Limnophilinae, Limoniinae and Chioneinae are considered non-monophyletic. The study allowed a reconstruction of the possible ground plan condition of selected features of the adult male morphology of crane flies. The genera/subgenera Epiphragma (Epiphragma), Acantholimnophila, Shannonomyia, Limnophila (Arctolimnophila), Eloeophila, Conosia, Polymera, Polymera (Polymerodes), Prionolabis, Eutonia, Phylidorea (Phylidorea), Metalimnophila, Gynoplistia (Cerozodia), Gynoplistia (Dirhipis), Nothophila, Pseudolimnophila (Pseudolimnophila), Pilaria and Ulomorpha are considered monophyletic, but in general are defined by combinations of very homoplastic character states. Two Temperate Gondwanan clades, (Tonnoirella + (Edwardsomyia + (Tinemyia + (Rhamphophila + (Nothophila))))) and ((Notholimnophila + Bergrothomyia) + (Mesolimnophila + (Chilelimnophila + Ctenolimnophila))) are recovered. The genera Limnophila, Neolimnomyia, Gynoplistia (sensu lato) and Hexatoma (sensu lato) are considered non-monophyletic. The systematic position and some morphological characters of ‘problematic’ taxa, such as Dactylolabis, Elephantomyia, Helius and Atarba are discussed on the light of the proposed phylogeny and the analysis of the characters. Character states are richly illustrated. A detailed study of the morphology of the male genitalia is made, and several genera and species have the morphology of the male genitalia illustrated for the first time.


2020 ◽  
Vol 190 (2) ◽  
pp. 654-708
Author(s):  
Bruno V B Rodrigues ◽  
Cristina A Rheims

Abstract Prodidominae was recently re-established as a subfamily of Gnaphosidae, comprising 316 species placed in 33 genera. In this study, we conduct a cladistic analysis including 59 species of Prodidominae and 32 outgroup species. The matrix is composed of 291 morphological characters and the data are analysed under the parsimony criterion, using differing weighting regimes. Prodidominae is not recovered as monophyletic, because Anagrina did not arise within the subfamily. Cryptotoerithus, Molycria, Myandra, Nomindra, Wesmaldra and Wydundra arise to form a clade. Thus, we re-establish Molycriinae as a distinct subfamily in Gnaphosidae, sister to Prodidominae. We redefine the limits of Prodidominae to include the genera Austrodomus, Brasilomma, Caudalia, Chileomma, Chileuma, Chilongius, Eleleis, Indiani, Katumbea, Lygromma, Lygrommatoides, Moreno, Namundra, Neozimiris, Nopyllus, Paracymbiomma, Plutonodomus, Prodidomus, Purcelliana, Theuma, Theumella, Tivodrassus, Tricongius, Zimirina and Zimiris. Species of these genera share the presence of anterior lateral spinnerets with pyriform gland spigots associated with patches of long setae and the presence of a large protrusion between coxae IV with erect setae and unsclerotized margins. In addition, we propose three new synonymies: Oltacloea as a junior synonym of Tricongius, and Prodida as junior synonym of Prodidomus. Lygromma ybyguara is transferred to Tricongius.


Zootaxa ◽  
2018 ◽  
Vol 4399 (4) ◽  
pp. 451
Author(s):  
FERNANDO HENRIQUE CARNIMEO ◽  
FERNANDO BARBOSA NOLL

The Neotropical thynnine genus Scotaena is revised and a cladistic analysis is presented. The analysis, conducted from 75 morphological characters of 31 terminal taxa, returned a single tree under equal weighting. The monophyly of Scotaena was not recovered. Three new genera and five new species are described: Kaysara gen. nov., Pseudoscotaena gen. nov. and Pampathynnus gen. nov., Scotaena reversa sp. nov., Kaysara laterolata sp. nov., Kaysara apiciconcava sp. nov., Kaysara marginoplicata sp. nov. and Kaysara levicrenata sp. nov. Three species are transferred to other genera as follows: Eucyrtothynnus rosenbergi (Turner, 1910) comb. nov., Glottynoides genisei Kimsey, 1991 comb. nov., Ornepetes clypearis Durán-Moya, 1941 comb. nov. Scotaena now comprises four species: S. trifasciata Klug, 1810; S. horni (Turner, 1927); S. vetusta Turner, 1909; and S. reversa. An identification key and geographical distribution maps for the studied species are also provided. 


Zootaxa ◽  
2020 ◽  
Vol 4873 (1) ◽  
pp. 1-132 ◽  
Author(s):  
ANDRE MORI ◽  
ROGERIO BERTANI

The genera Psalistops Simon, 1889, Trichopelma, Simon, 1888 and Cyrtogrammomma Pocock, 1895 are revised and included in cladistics analyses including almost all species of these genera. In order to test previous morphological hypotheses on the relationships of Barychelidae, Paratropididae and Theraphosidae and because of the controversial taxonomic position of Psalistops and Trichopelma, a set of terminal taxa representing all subfamilies of Paratropididae (Paratropidinae, Glabropelmatinae), Barychelidae (Barychelinae, Sasoninae, Trichopelmatinae) and most theraphosid subfamilies were included, as well as a diplurid, a nemesiid, and a pycnothelid, the later used to root the cladogram. The matrix with 66 terminal taxa, 2 continuous and 93 discrete characters was analysed with TNT 1.5. We found that Trichopelmatinae is not a monophyletic group, and Psalistops is transferred to Theraphosidae, as well as the barychelid genus Cyrtogrammomma and the paratropidid genus Melloina Brignoli. Cyrtogrammomma was retrieved as the sister group of Trichopelma, and Melloina as the sister group of Holothele Karsch. Psalistops was retrieved as the sister group of Reichlingia Rudloff, and the clade with these two genera is the most basal in Theraphosidae. Barychelidae was found to be monophyletic and the sister group of Theraphosidae. Paratropididae was retrieved as the sister group of Barychelidae + Theraphosidae. The relationship and possible synapomorphies of the three families are herein discussed.                This is the first time since Raven (1985) that representatives of all barychelid (Barychelinae, Sasoninae, Trichopelmatinae), paratropidid (Paratropidinae, Glabropelmatinae) and most theraphosid subfamilies have been included in a morphological cladistic analysis.                Psalistops comprises two species, P. melanopygius Simon, 1889 (type species) and P. colombianus sp. nov. Psalistops montigena Simon, 1889, P. tigrinus Simon, 1889 and P. zonatus Simon, 1889 are synonymized with P. melanopygius Simon, 1889. Psalistops fulvus Bryant, 1948, P. hispaniolensis Wunderlich, 1988 (fossil), P. maculosus Bryant, 1948, P. venadensis Valerio, 1986 and P. steini (Simon, 1889) are transferred to Trichopelma. Psalistops gasci Maréchal, 1996 is transferred to Hapalopus Ausserer (Theraphosidae); P. opifex (Simon, 1889) and P. solitarius (Simon, 1889) are transferred to Schismatothele Karsch, 1879 (Theraphosidae). Schismatothele solitarius (Simon, 1889) n. comb. is synonymized with Schismatothele lineata Karsch, 1879, n. syn. Psalistops nigrifemuratus Mello-Leitão, 1939 is probably a nemesiid or pycnothelid, and herein considered as nomen dubium in Pycnothelidae. Trichopelma comprises 22 species: Trichopelma nitidum Simon, 1888 (type species), T. coenobita (Simon, 1889), T. steini (Simon, 1889), T. affine (Simon, 1892), T. cubanum (Simon, 1903), T. maculatum (Banks, 1906), T. zebra (Petrunkevitch, 1925), T. banksia Özdikmen & Demir, 2012, T. insulanum (Petrunkevitch, 1926), T. fulvus (Bryant, 1948) n. comb., T. laselva Valerio, 1986, T. venadensis (Valerio, 1986) n. comb., T. huffi sp. nov., T. gabrieli sp. nov., T. tostoi sp. nov., T. goloboffi sp. nov., T. juventud sp. nov., T. laurae sp. nov., T.bimini sp. nov., T. loui sp. nov., T. platnicki sp. nov., and T. hispaniolensis Wunderlich, 1988 n. comb. (fossil). Trichopelma maculosus (Bryant, 1948) n. comb. is synonymized with P. fulvus Bryant, 1948; T. corozalis (Petrunkevitch, 1929) is synonymized with T. insulanum (Petrunkevitch, 1926). Trichopelma astutum Simon, 1889 is transferred to Euthycaelus Simon, 1889, and T. maddeni Esposito & Agnarsson, 2014 to Holothele Karsch, 1879 (Theraphosidae). Trichopelma flavicomum Simon, 1891 is transferred to Neodiplothele (Barychelidae, Sasoninae). The species T. illetabile Simon, 1888, T. spinosum (Franganillo, 1926), T. scopulatum (Fischel, 1927) and T. eucubanum Özdikmen & Demir, 2012 are considered as nomina dubia. Cyrtogrammomma comprises two species: C. monticola Pocock, 1895 (type species) and C. raveni sp. nov.


Zootaxa ◽  
2019 ◽  
Vol 4551 (2) ◽  
pp. 101 ◽  
Author(s):  
K. J. DAVID ◽  
S. RAMANI

The tribe Dacini comprising four genera, namely Bactrocera Macquart, Dacus Fabricius, Monacrostichus Bezzi and Zeugodacus Hendel, is a derived lineage in Tephritidae. It is one of the most economically important tribes in Tephritidae harbouring several species of quarantine concern across the world. We describe two new species of Bactrocera Macquart, B. (Parazeugodacus) conica David & Ramani, sp. n. & B. (B.) prabhui David, sp. n. from India. Postabdominal structures of males and/or females of 23 species of Bactrocera, 16 species of Zeugodacus and 8 species of Dacus from India are illustrated and described for the first time, which revealed similarities between Dacus and Zeugodacus with respect to epandrial shape and praeputium patterning. Bactrocera is unique in possessing oval shaped epandrium and an unpatterned praeputium. An analysis of phylogenetic relationships between three genera of the tribe Dacini from India based on morphological characters has been attempted for the first time. Cladistic analysis employing 51 characters of 62 species in Dacini, with seven species as outgroups revealed the monophyly of Dacini, Bactrocera and Dacus with supporting nonhomplasious synapomorphies. Ichneumonopsis Hardy, often included in the Gastrozonini, does not possess any synapomorphies of Dacini, eventhough it appeared at the base of the Dacini clade. Zeugodacus was retrieved as a monophyletic sister-group to Dacus based solely on a single homoplasious host plant character, with weak statistcal support. 


2011 ◽  
Vol 25 (6) ◽  
pp. 490 ◽  
Author(s):  
Edilson Caron ◽  
Cibele S. Ribeiro-Costa ◽  
Alfred F. Newton

Rove beetles of the genus Piestus Gravenhorst, 1806 are commonly captured under the bark of or inside decaying logs from Neotropical forests. Piestus belongs to the subfamily Piestinae, historically an ill-defined dumping-ground for Staphylinidae defined by plesiomorphic characters, but which has gradually been restricted in concept and currently includes only six additional extant genera worldwide. Piestinae in this restricted sense has been considered a probably monophyletic subfamily, but its status and phylogenetic position, as a possible sister-group of Osoriinae within the recently proposed Oxyteline group of staphylinid subfamilies, are uncertain and need confirmation. The main aim of the present study was to provide a morphological cladistic analysis and complete taxonomic revision of Piestus, which, as the type and most speciose genus of Piestinae, is critical for future phylogenetic studies involving the subfamily. In our study, the monophyly of Piestus is established and phylogenetic relationships among its species are proposed based on 70 adult morphological characters. Piestus is supported by 11 synapomorphies and high branch support. All species of Piestus are revised and the genus is redefined. The genus contains 43 species, including 13 species described here for the first time. The previously proposed subgenera Antropiestus Bernhauer, 1917, Eccoptopiestus Scheerpeltz, 1952, Elytropiestus Scheerpeltz, 1952, Lissopiestus Scheerpeltz, 1952, Piestus s. str., Trachypiestus Scheerpeltz, 1952 and Zirophorus Dalman, 1821 have not been confirmed, as they were found to be poly- or paraphyletic, or are here removed from Piestus, and therefore subgenera are not used. The main taxonomic changes are as follows. Lissopiestus, syn. nov. is proposed as new synonym of Eleusis Laporte, 1835 and its species, E. interrupta (Erichson, 1840), comb. rest., is transferred again to that genus. Antropiestus, syn. nov. and Eccoptopiestus, syn. nov. are proposed as new synonyms of Hypotelus Erichson, 1839 and their species, H. laevis (Solsky, 1872), comb. nov. and H. andinus (Bernhauer, 1917), comb. nov., are transferred to Hypotelus. Fourteen new synonymies are proposed (valid species listed first): P. lacordairei Laporte, 1835 = Z. furcatus Sharp, 1887, syn. nov.; P. capricornis Laporte, 1835 = P. frontalis Sharp, 1876, syn. nov.; P. pennicornis Fauvel, 1864 = P. plagiatus Fauvel, 1864, syn. nov.; P. rectus Sharp, 1876, syn. nov.; P. pygialis Fauvel, 1902, syn. nov.; P. surinamensis Bernhauer, 1928, syn. nov.; P. minutus Erichson, 1840 = P. nigrator Fauvel, 1902, syn. nov.; P. sulcatus Gravenhorst, 1806 = P. sanctaecatharinae Bernhauer, 1906, syn. nov.; P. condei Wendeler, 1955, syn. nov.; P. gounellei Fauvel, 1902 = P. wasmanni Fauvel, 1902, syn. nov.; P. mexicanus Laporte, 1835 = P. alternans Sharp, 1887, syn. nov.; P. aper Sharp, 1876 = P. schadei Scheerpeltz, 1952, syn. nov.; P. angularis Fauvel, 1864 = P. crassicornis Sharp, 1887, syn. nov.; H. andinus (Bernhauer, 1917) = P. strigipennis Bernhauer, 1921, syn. nov. One species is revalidated: P. fronticornis (Dalman, 1821), stat. rev., and one synonym is restored: P. penicillatus (Dalman, 1821) = P. erythropus Erichson, 1840, syn. rest. Neotypes are designated for P. lacordairei Laporte, 1835 and Oxytelus bicornis Olivier, 1811, and lectotypes are designated for P. puncticollis Fauvel, 1902, P. capricornis variety muticus Fauvel, 1902, P. zischkai Scheerpeltz, 1951, P. pennicornis Fauvel, 1864, P. plagiatus Fauvel, 1864, P. pygmaeus Laporte, 1835, P. niger Fauvel 1864, P. minutus Erichson, 1840, P. nigratror Fauvel, 1902, P. sulcatus Gravenhorst, 1806, P. sanctaecatharinae Bernhauer, 1906, P. sulcipennis Scheerpeltz, 1952, P. aper Sharp, 1876, P. schadei Scheerpeltz, 1952 and P. andinus Bernhauer, 1917.


Phytotaxa ◽  
2016 ◽  
Vol 262 (1) ◽  
pp. 1 ◽  
Author(s):  
MARCELO REGINATO

A taxonomic monograph of a re-circumscribed Leandra sect. Leandra is presented. The new circumscription is based on a previous phylogenetic hypothesis, and diagnostic morphological characters are discussed. Four new combinations to Leandra are proposed, one from Clidemia (L. capilliflora) and three from Ossaea (L. capitata, L. cogniauxii and L. loligomorpha). Additionally, eight species are treated as synonyms for the first time, and 15 lectotypes are designated. A review of the 17 recognized species, including descriptions, synonymy, illustrations and distribution maps, is provided. This work also includes an overview of general morphology, leaf and flower anatomy, phenology and geographical distribution. Species with a history of taxonomic problems and/or with distinctive morphotypes are further investigated with morphometrics tools.


Sign in / Sign up

Export Citation Format

Share Document